(2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran

Base Information

• Chemical Name: (2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran
• CAS No.: 876133-09-4
• Molecular Formula: C₂₅H₃₇IO₈Si
• Molecular Weight: 620.554
• Mol file: 876133-09-4.mol

Synonyms:(2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran

Chemical Property of (2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran

There total 8 articles about (2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

(2S,3R,4R,5S,6S)-5-hydroxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran (876133-08-3) + tert-butyldimethylsilyl chloride (18162-48-6) → (2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran (876133-09-4)

Guidance literature:

With 1H-imidazole; In dichloromethane; at 20 ℃; for 50h;

DOI:10.1055/s-2005-918474

Reference yield:

(2R,4aR,6S,7R,8R,8aR)-6-methoxy-8-(3-oxobutylcarbonyloxy)-2-phenyl-7-phenylcarbonyloxyperhydropyrano[3,2-d][1,3]dioxine (876133-06-1) → (2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran (876133-09-4)

Guidance literature:

Multi-step reaction with 3 steps

1: H₂ / Pd/C / ethyl acetate / 12 h / 20 °C

2: 53.00 g / PPh₃; I₂; imidazole / tetrahydrofuran / 1 h / 20 °C

3: 95 percent / imidazole / CH₂Cl₂ / 50 h / 20 °C

With 1H-imidazole; hydrogen; iodine; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate;

DOI:10.1055/s-2005-918474

Reference yield:

(2R,4aR,6S,7R,8R,8aR)-8-hydroxy-6-methoxy-2-phenyl-7-phenylcarbonyloxyperhydropyrano[3,2-d][1,3]dioxine (99265-94-8) → (2S,3R,4R,5S,6S)-5-tert-butyldimethylsilyloxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran (876133-09-4)

Guidance literature:

Multi-step reaction with 4 steps

1: 143.0 g / dicyclohexylcarbodiimide; DMAP / CH₂Cl₂ / 17 h / 20 °C

2: H₂ / Pd/C / ethyl acetate / 12 h / 20 °C

3: 53.00 g / PPh₃; I₂; imidazole / tetrahydrofuran / 1 h / 20 °C

4: 95 percent / imidazole / CH₂Cl₂ / 50 h / 20 °C

With 1H-imidazole; dmap; hydrogen; iodine; dicyclohexyl-carbodiimide; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate;

DOI:10.1055/s-2005-918474

upstream raw materials:

(2S,3R,4R,5S,6S)-5-hydroxy-6-iodomethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran

tert-butyldimethylsilyl chloride

(2S,3R,4R,5R,6R)-5-hydroxy-6-hydroxymethyl-2-methoxy-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran

(2R,4aR,6S,7R,8R,8aR)-6-methoxy-8-(3-oxobutylcarbonyloxy)-2-phenyl-7-phenylcarbonyloxyperhydropyrano[3,2-d][1,3]dioxine

Downstream raw materials:

(2S,3R,4R,5R,6R)-5-tert-butyldimethylsilyloxy-2-methoxy-6-methyl-4-(3-oxobutylcarbonyloxy)-3-phenylcarbonyloxytetrahydro-2H-pyran

(2S,3R,4R,5R,6R)-4-hydroxy-2-methoxy-6-methyl-3-phenylcarbonyloxy-5-tert-butyldimethylsilyloxytetrahydro-2H-pyran

(2S,3R,4S,5S,6R)-4-azido-5-tert-butyldimethylsilyloxy-2-methoxy-6-methyl-3-phenylcarbonyloxytetrahydro-2H-pyran

(2S,3R,4R,5R,6R)-5-tert-butyldimethylsilyloxy-2-methoxy-6-methyl-3-phenylcarbonyloxy-4-trifluoromethylsulfonyloxytetrahydro-2H-pyran